S38N (p.Ser38Asn) variant of ACADM (P11310)
S38N (p.Ser38Asn) in ACADM (P11310) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
S38N (p.Ser38Asn) variant details
- p.Ser38Asn
- TOPMed rs1006082856
- gnomAD rs1006082856
- Missense
- Variant Prioritization Score for Impact Estimate 0.502
- REVEL 0.37
- CADD 15.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available